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ABSTRACT: Purpose
Pheochromocytoma (PCC) and paraganglioma (PGL) (PPGL) are rare neuroendocrine tumors, and data on managing these conditions in children and adolescents are lacking. The objective of this study was to demonstrate the clinical presentation and treatment outcomes in children and adolescents with PPGL in a single tertiary care center in Korea.Methods
This retrospective study included 23 patients diagnosed with PCC (n = 14) and PGL (n = 9) before the age of 21 at Samsung Medical Center (from June 1994 to June 2019). We describe age, gender, family history, clinical characteristics, laboratory findings, pathologic findings, therapeutic approaches, and treatment outcomes.Results
Of the 23 patients, 14 had PCC and nine had PGL. The median age at diagno
SUBMITTER: Park H
PROVIDER: S-EPMC7879705 | biostudies-literature | 2020
REPOSITORIES: biostudies-literature